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High density marker panels, SNPs prioritizing and accuracy of genomic selection
BACKGROUND: The availability of high-density (HD) marker panels, genome wide variants and sequence data creates an unprecedented opportunity to dissect the genetic basis of complex traits, enhance genomic selection (GS) and identify causal variants of disease. The disproportional increase in the num...
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| Publicat a: | BMC Genet |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5756446/ https://ncbi.nlm.nih.gov/pubmed/29304753 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12863-017-0595-2 |
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